Investigation of the Clinical Performance of Silicone Hydrogel Contact Lenses During Continuous Wear
Not Applicable
Completed
- Conditions
- Myopia
- Registration Number
- NCT00346593
- Lead Sponsor
- University of Melbourne
- Brief Summary
The primary purpose of this study is to investigate the clinical performance of a new silicone hydrogel contact lens during continuous wear (up to 30 nights) over a period of 24 months.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- All
- Target Recruitment
- Not specified
Inclusion Criteria
- Has had an oculo-visual examination in the last 2 years.
- Is correctable to at least 6/7.5 distance visual acuity in each eye with spherical contact lenses.
- Is a current soft contact lens wearer.
- Has no clinically significant anterior eye findings.
- Has no other active ocular disease.
Exclusion Criteria
- Has any systemic disease that might interfere with contact lens wear
- Is using any systemic or topical medications that will affect ocular health.
- Has any pre-existing ocular irritation that would preclude contact lens fitting.
- Has any ocular pathology or severe insufficiency of lacrimal secretion (dry eyes) that would affect the wearing of contact lenses.
- Has undergone corneal refractive surgery.
- Is pregnant, lactating or planning a pregnancy.
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- SINGLE_GROUP
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method
Trial Locations
- Locations (1)
Clinical Vision Research Australia
🇦🇺Carlton, Victoria, Australia